Grants Funded
Grant applicants for the 2024 cycle requested a total of nearly $3 million dollars. The PSF Study Section Subcommittees of Basic & Translational Research and Clinical Research evaluated more than 100 grant applications on the following topics:
The PSF awarded research grants totaling over $650,000 dollars to support more than 20 plastic surgery research proposals.
ASPS/PSF leadership is committed to continuing to provide high levels of investigator-initiated research support to ensure that plastic surgeons have the needed research resources to be pioneers and innovators in advancing the practice of medicine.
Research Abstracts
Search The PSF database to have easy access to full-text grant abstracts from past PSF-funded research projects 2003 to present. All abstracts are the work of the Principal Investigators and were retrieved from their PSF grant applications. Several different filters may be applied to locate abstracts specific to a particular focus area or PSF funding mechanism.
Harnessing Heterotopic Ossification for Bone Regeneration
Anand Kumar MD
2012
University of Pittsburgh
Pilot Research Grant
Cranio / Maxillofacial / Head and Neck, Tissue Engineering
It is estimated that 50-60% of all extremity injuries in the US military are complicated by delayed heterotopic ossification (HO). Although not fatal, the considerable morbidity associated with HO includes pain, inability to fit amputation prosthesis properly, and a grotesque appearance to the extremity that prevents proper psycho/social rehabilitation. The estimated 50,000-battlefield injuries secondary to Operation Iraqi and Enduring Freedom has increased awareness of this entity beyond orthopedic surgeons who have traditional treated HO. There is evidence that muscle derived progenitor cells (MDC)s have osteogenic potential and are the source of the structurally sound mature endochondrial bone formed in HO. We seek to establish a murine translational HO model to harness MDC mediated osteogenesis. Although the initial goals of my research include the understanding and inhibition of the processes of HO, the information that will be gained in pursuit of these goals should be directly applicable to strategies designed to enhance or induce bone regeneration. If we understand how to stop bone from forming, we may better understand how to initiate bone formation. Our laboratory has established a technique for isolating MDCs from murine muscle. We have also fabricated 3D cell cultures and gathered preliminary data that suggests the osteogenic potential of these MDCs. In this study, we hypothesize that MDCs isolated from murine muscle will display in vitro osteoegenic differentiation in response to osteoinductive factors. We expect cyclical motion and inflammatory mediators (both being intrinsic to the HO process) to further enhance the in vitro osteogenic differentiation of MDCs. Finally, we hypothesize that osteoinduced MDCs will promote in vivo bone growth when implanted into heterotopic locations or into large orthotopic defects in syngeneic animals.
